HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 653981Erstellt: 26. Oktober 2026
Chlorotrimethylsilane → HCID 15126108, Verbindung
https://huagongshe.com/reaction/653981
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | Hexamethyldisilazane | HCID 13838 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1-O-Acetyl-5-O-t-butyldiphenylsilyl-4-thio-2,3-dideoxyribofuranose | HCID 15126098 | — |
| Edukt | Potassium perfluorobutanesulfonate | HCID 23675274 | — |
| Edukt | Cytosine | HCID 178418229 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 15126108 | HCID 15126108 | — |
Reaktionsschritte
A mixture of 10 (0.26 g, 0.63 mmol), cytosine (0.105 g, 0.95 mmol), and potassium nonafluorobutanesulfonate (0.77 g, 2.3 mmol) was suspended in 12 mL dry acetonitrile under nitrogen. HMDS (0.135 mL, 0.63 mmol) and TMS-Cl (0.37 mL, 2.9 mmol) were added sequentially via syringe and the reaction stirred at 25° C. overnight. The reaction was poured into a mixture of 20 mL dichloromethane and 15 mL saturated NaHCO3 and shaken. The organic phase was dried (MgSO4) and concentrated in vacuo. The anomeric mixture was separated by preparative TLC with 7.5% MeOH/CHCl3 with an ammonia atmosphere: yield of β-anomer, 78 mg and 117 mg of the α-anomer to afford total yield of 195 mg (66.5%); FAB MS 466 (M+H)+ ; 1H NMR (CDCl3) of α/β anomer, δ 8.12 (d, 1, 6-H), 7.7 (m, 4, ArH), 7.4 (m, 6, ArH), 6.32 (m, 1, 1'-H), 5.9-5.3 (hump, 1, NH2), 5.75 (d, 1, 5-H), 5.45 (d, 1, 5-H), 3.75 (m, 3, 4'-Hα,β 's, 3'-Hα,β 's).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05128458 |
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| Quelldatensatz | uspto-grants-1992_07 |
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| ORD ID | ord-e369a01e7e4949d5a42ef03f07094859 |
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| Quellennotiz | uspto-grants-1992_07 |
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